Variant report

Variant	rs4813538
Chromosome Location	chr20:24763641-24763642
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr20:24763298..24765600-chr20:24898179..24900035,23	MCF-7	breast:
2	chr20:24763560..24765112-chr20:24971515..24973811,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000101474	Chromatin interaction

Extended variants
information (count: 43 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs11698988	0.90[ASN][1000 genomes]
rs12480651	0.97[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs226664	0.82[CHB][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs4813539	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4813540	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs4815303	0.88[EUR][1000 genomes]
rs4815308	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4815312	0.98[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs4815315	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs56103836	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs6036904	0.90[AFR][1000 genomes];0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6036910	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6036911	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6049933	0.86[AFR][1000 genomes];0.87[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs6049943	0.83[AFR][1000 genomes];0.90[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs6049956	0.85[AFR][1000 genomes];0.95[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs6049971	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6049976	1.00[CEU][hapmap];0.89[YRI][hapmap];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs6049977	0.98[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs6049978	1.00[CEU][hapmap];0.84[YRI][hapmap];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs6049983	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs6076276	0.90[ASN][1000 genomes]
rs6076277	0.90[ASN][1000 genomes]
rs6083620	0.90[ASN][1000 genomes]
rs61059580	0.98[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs6114868	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6132765	0.90[ASN][1000 genomes]
rs7264934	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7271933	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs73335420	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs73335440	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs73335460	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs73612620	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs743191	0.98[AMR][1000 genomes];0.97[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3332519	chr20:24535099-24815615	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv1061412	chr20:24629468-24887869	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv544216	chr20:24629468-24887869	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv1061281	chr20:24711635-24815107	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
5	nsv544217	chr20:24711635-24815107	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
6	nsv912825	chr20:24715544-24813345	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
7	nsv1061455	chr20:24733120-24861801	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Genic enhancers Bivalent/Poised TSS	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
8	nsv544218	chr20:24733120-24861801	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
9	nsv1059270	chr20:24741923-24787243	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:21 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:24757800-24766600	Enhancers	Fetal Thymus	thymus
2	chr20:24758400-24766800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr20:24758600-24763800	Enhancers	Fetal Muscle Leg	muscle
4	chr20:24758800-24767400	Enhancers	Primary hematopoietic stem cells short term culture	blood
5	chr20:24759800-24767000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr20:24761400-24764000	Enhancers	Brain Hippocampus Middle	brain
7	chr20:24761400-24765200	Weak transcription	Primary T cells from cord blood	blood
8	chr20:24762200-24767000	Enhancers	Dnd41	blood
9	chr20:24762400-24765400	Weak transcription	GM12878-XiMat	blood
10	chr20:24762600-24764000	Enhancers	Fetal Lung	lung
11	chr20:24762800-24766400	Enhancers	Thymus	Thymus
12	chr20:24762800-24766600	Enhancers	Primary hematopoietic stem cells	blood
13	chr20:24763000-24764000	Enhancers	Fetal Stomach	stomach
14	chr20:24763400-24764000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr20:24763400-24764000	Enhancers	NH-A	brain
16	chr20:24763400-24765800	Weak transcription	Brain Substantia Nigra	brain
17	chr20:24763400-24767000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr20:24763600-24763800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr20:24763600-24763800	Enhancers	Brain Inferior Temporal Lobe	brain
20	chr20:24763600-24763800	Enhancers	Fetal Kidney	kidney
21	chr20:24763600-24764400	Enhancers	Fetal Muscle Trunk	muscle

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